Author:
Goodship J,Cross I,Scambler P,Burn J
Subject
Genetics (clinical),Genetics
Reference17 articles.
1. Deletions and microdeletions of 22q1 1.2 in velo-cardio-facial syndrome;Driscoll, D.A.; Spinner, N.B.; Budarf, M.L.;AmJ Med Genet,1992
2. Prevalence of 22q1 1 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis;Driscoll, D.A.; Salvin, J.; Sellinger, B.;J7 Med Genet,1993
3. Microdeletions of chromosome 22qll in patients with congenital conotruncal cardiac defects;Goldmuntz, E.; Driscoll, D.; Budarf, M.L.;J Med Genet,1993
4. Deletions within chromosome 22q 1I in familial congenital heart disease;Wilson, D.I.; Goodship, J.A.; Burn, J.; Cross, I.E.; Scambler, P.J.;Lancet,1992
5. Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus;Scambler, P.J.; Kelly, D.; Lindsay, E.;Lancet,1992
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